Camntech, Ltd. is one of 479 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Camntech, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MOTION WATCH AND PRO-DIARY, ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603
2
Total
2
Cleared
0
Denied
Camntech, Ltd. is a medical device manufacturer with a manufacturing facility in Papworth Everard, Cambridgeshire, United Kingdom. The company specialized in wearable monitoring and cardiovascular diagnostic devices.
Camntech received 2 FDA 510(k) clearances from 2 total submissions between 2010 and 2014. The company's primary focus was cardiovascular devices, including ambulatory monitoring systems and activity-based diagnostic platforms. A secondary area of activity included neurology-related monitoring devices.
This company is now inactive, with no FDA 510(k) clearances recorded in more than five years. The regulatory record presented here is historical and reflects the company's cleared device portfolio during its active period.
For detailed information on specific device names, product codes, and individual clearance dates, please review the complete 510(k) clearance database entry.
FDA 510(k) Regulatory Record - Camntech, Ltd.
2 devices